Canonical Allele Identifier: CA2611246992

Gene: HTRA1

Linked Data

• gnomAD v4: 10-122508589-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122508589C>T , CM000672.2:g.122508589C>T	GRCh38
NC_000010.10:g.124268105C>T , CM000672.1:g.124268105C>T	GRCh37
NC_000010.9:g.124258095C>T	NCBI36
NG_011554.1:g.52065C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.1006-67C>T MANE Select	ENSP00000357980.3:n.1006-67C>T
ENST00000648167.1:c.688-67C>T	ENSP00000498033.1:n.688-67C>T
ENST00000368984.7:c.1006-67C>T	ENSP00000357980.3:n.1006-67C>T
ENST00000420892.1:c.229-67C>T	ENSP00000412676.1:n.229-67C>T
NM_002775.4:c.1006-67C>T	NP_002766.1:n.1006-67C>T
NM_002775.5:c.1006-67C>T MANE Select	NP_002766.1:n.1006-67C>T